Host-microbiota interactions in inflammatory bowel disease

被引:33
|
作者
Caruso, Roberta [1 ,2 ]
Lo, Bernard C. [1 ,2 ]
Nunez, Gabriel [1 ,2 ]
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Rogel Canc Ctr, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
REGULATORY T-CELLS; GENOME-WIDE ASSOCIATION; INTESTINAL DENDRITIC CELLS; INVASIVE E. COLI; CROHNS-DISEASE; ULCERATIVE-COLITIS; COMMENSAL BACTERIA; PANETH CELLS; IMMUNE-RESPONSES; MUC2; MUCIN;
D O I
10.1038/s41577-019-0268-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This Review describes the breakdown of 'mucosal firewalls' in patients with inflammatory bowel disease, involving immunological pathways that regulate microbial recognition and killing, immune responses to microorganisms and the reinforcement of the intestinal barrier. The mammalian intestine is colonized by trillions of microorganisms that have co-evolved with the host in a symbiotic relationship. The presence of large numbers of symbionts near the epithelial surface of the intestine poses an enormous challenge to the host because it must avoid the activation of harmful inflammatory responses to the microorganisms while preserving its ability to mount robust immune responses to invading pathogens. In patients with inflammatory bowel disease, there is a breakdown of the multiple strategies that the immune system has evolved to promote the separation between symbiotic microorganisms and the intestinal epithelium and the effective killing of penetrant microorganisms, while suppressing the activation of inappropriate T cell responses to resident microorganisms. Understanding the complex interactions between intestinal microorganisms and the host may provide crucial insight into the pathogenesis of inflammatory bowel disease as well as new avenues to prevent and treat the disease.
引用
收藏
页码:411 / 426
页数:16
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